نتایج جستجو برای: bisindolyl methanes

تعداد نتایج: 287  

Journal: :The Journal of organic chemistry 2016
Jia-Bin Han Hua-Li Qin Su-Hong Ye Lei Zhu Cheng-Pan Zhang

Construction of difluoromethylthioethers (2) and difluorobis(arylthio)methanes (3) from RSX (X = SR, Cl, SO2Ph) and TMSCF2H in the absence of transition metals has been explored. The reaction is dramatically influenced by the nature of the base and the molar ratio of the reactants. Reactions between RSX and TMSCF2H in the presence of CsF provided 2 in good yields, whereas the reaction of RSX wi...

Journal: :journal of sciences, islamic republic of iran 2013
n. seyedi

in this work, a green, simple and highly efficient procedure for the synthesis of bis(indolyl)methanes is described. the condensation of indoles with carbonyl compounds catalyzed by citric acid in water affords bis(indolyl)methanes in high yields and relatively short reaction times. the advantages of this method are using of water as a low cost solvent and efficient recyclability of the catalyst.

2003
Ji-Tai Li Xiao-Hui Zhang Ya-Li Song

Synthesis of bis(indol-3-yl)methanes catalyzed by silicotungstic acid (SiO212WO324H2O) was carried out in 50-97% yield within 15-120 min in EtOH at r. t. under ultrasound irradiation.

Journal: :Journal of the American Chemical Society 2012
Joseph B Gianino Brandon L Ashfeld

A titanocene-catalyzed multicomponent coupling to provide diarylethynyl methanes is described. By combining the multifunctionality of Cp(2)TiCl(2) with the traceless dielectrophilicity of aryl aldehydes, all-carbon tertiary centers are obtained in 55-99% yield.

2017
Pauline Chaignaud Bruno Maucourt Marion Weiman Adriana Alberti Steffen Kolb Stéphane Cruveiller Stéphane Vuilleumier Françoise Bringel

Bacterial adaptation to growth with toxic halogenated chemicals was explored in the context of methylotrophic metabolism of Methylobacterium extorquens, by comparing strains CM4 and DM4, which show robust growth with chloromethane and dichloromethane, respectively. Dehalogenation of chlorinated methanes initiates growth-supporting degradation, with intracellular release of protons and chloride ...

Journal: :Bioorganic & medicinal chemistry letters 2010
C Praveen P DheenKumar D Muralidharan P T Perumal

An improved and practical synthesis of substituted quinolines and bis(indolyl)methanes was achieved under microwave condition using Zn(OTf)(2) as catalyst. The synthesized compounds have been screened for antimicrobial and antioxidant activities.

Journal: :The Journal of chemical physics 2011
Mark T Oakley Hainam Do Jonathan D Hirst Richard J Wheatley

We present pair potentials for fluorinated methanes and their dimers with CO(2) based on ab initio potential energy surfaces. These potentials reproduce the experimental second virial coefficients of the pure fluorinated methanes and their mixtures with CO(2) without adjustment. Ab initio calculations on trimers are used to model the effects of nonadditive dispersion and induction. Simulations ...

Arman Rahmaninia Farhad Shirini, Manouchehr Mamaghani Masoumeh Abedini

Benzyltriphenylphosphonium bromide (BTPB) has been applied as an efficient catalyst for the preparation of bis(indolyl)methanes (BIMs) via electrophilic substitution of indoles with aldehydes in the absence of solvent.

2013
Uday Kumar

A novel synthetic methodology for the synthesis of Bis(indolyl)methanes by using catalytic amount of ferric triflate was described Introduction Bis(indolyl)methanes consists two substituted indole units in the molecule. Bis indole derivatives are reported to exhibit a wide spectrum of pharmacological activities such as cytotoxic, antitumor antimicrobial [1] and antiactivities. [2] For the past ...

Journal: :caspian journal of chemistry 0
heshmatollah alinezhad faculty of chemistry, mazandaran university, babolsar, iran asefeh hagh haghighi faculty of chemistry, mazandaran university, babolsar, iran

β-cyclodextrin sulfuric acid as a green lewis acid catalyst has been applied for the preparation of bis(indolyl)methanes, tris(indolyl)methanes and 3,3'-diindolyloxindole derivatives by the condensation of indoles with various carbonyl compounds in aqueous media with high to excellent yields.

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